Canonical Allele Identifier: PA2826200333
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 290957
ClinVar RCV Id: RCV000324352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182181.2:p.Pro258His
CA10606959
NM_001195252.2:c.773C>A